iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3677	snp	A/C	0.00806438	0.0629854	intron-variant	TOM1L2	GRCh38.p7	17:17868937	GGGAAAGAGGAAATC[A/C]TTTTTCTTACTAGAG	146691
rs745401	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901673	GGAACTGAAGACATG[C/T]AATAGAGCAAGATAA	146691
rs950966	snp	C/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17880434	GGAGAAAGTGTATGA[C/T]GTCTCTGTTGCTGGA	146691
rs998179	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17884458	AGTGAGACAGCTGGT[C/T]GACTGGTGATTAAGT	146691
rs1052299	snp	C/T	0.453697	0.14494	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847105	GTGACATTTGGCTTA[C/T]CAGCATTTGAGAAGG	146691
rs1108646	snp	C/T	0.495927	0.0449436	intron-variant	TOM1L2	GRCh38.p7	17:17848164	GCATCTCCTCAGTCC[C/T]CCATTGGTGGGCAAG	146691
rs1108648	snp	A/G	0.442655	0.159323	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847244	ATGCCTGAGAAGGTC[A/G]CTGAGCCAGGCAGAG	146691
rs1737972	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17893354	TAGGAAGAACCATGT[A/T]AGAGCTACGTGCGGG	146691
rs1737973	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17893310	CAGGGCAGGGGCCAA[A/C]TCTGGGTCAGGCGGA	146691
rs1759082	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17893299	CCAAATCTGGGTCAG[C/G]CGGAGCAAGGTAAGg	146691
rs1889014	snp	A/G	0.346147	0.230772			GRCh38.p7	17:17863851	caacaaaaGTGTAGT[A/G]TCCAccaggggtggt	146691
rs1889015	snp	C/T	0.0528381	0.153711			GRCh38.p7	17:17844512	GGAAAGGTGACCATC[C/T]GTCTGTCCTCCTGTC	146691
rs2236513	snp	G/T	0.476918	0.104919	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844052	TCTGCACTGTCGGCT[G/T]TGGGGACGTCTCACC	146691
rs2274893	snp	A/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17885030	AGGTGTTATTTCTCT[A/G]TCTCTTCTCCAAGGA	146691
rs2350977	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17899465	AAAGTTGGAGTGGAG[C/T]TGTTTGGAAGTTGGA	146691
rs3075551	snp	A/G	0.46875	0.121031	intron-variant	TOM1L2	GRCh38.p7	17:17894975	CATACATACATACAT[A/G]CATGCATGCATGCAT	146691
rs3075553	in-del	-/GCATGCAT	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17894994	catgcatgcatgcat[-/GCATGCAT]aaaataatgcacata	146691
rs3183702	snp	C/T	0.477004	0.104734	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843975	ACCCCAGAGACATTG[C/T]CTGTCAGCCCCTGAA	146691
rs3737121	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17849136	AGAACCAGCCTGCAC[C/T]GTTTTTGGAGTTTTC	146691
rs3737122	snp	A/G	0.105214	0.203807	intron-variant	TOM1L2	GRCh38.p7	17:17849078	CTAAAACATGTTTGA[A/G]TTTTTTGCTTTTGTT	146691
rs3737123	snp	A/G	0.136847	0.222927	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846794	TGTGGAGGGACTTGC[A/G]CTGGAGGTATTGCTC	146691
rs3744113	snp	C/T	0.44858	0.151875	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845331	AGGCCTCTCCAATGA[C/T]GCCTGGCAACCAGCT	146691
rs3744114	snp	C/T	0.0379877	0.132479	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846472	TACATGTTACCAGCC[C/T]CTAGCTGCTCTGCCT	146691
rs3744115	snp	A/G	0.453575	0.145111	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846508	CAGGATCAGCTTGGG[A/G]AGAGAGTATAAATTG	146691
rs4077198	snp	A/G	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17931249	TGGAGAATTGGGGAA[A/G]TCTGTAGAAGAGGAA	146691
rs4077828	snp	A/T	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17930330	TGGTCTTAGGAAATG[A/T]CCAAATCAGAGACTC	146691
rs4244602	snp	A/G	0.392325	0.205532	intron-variant	TOM1L2	GRCh38.p7	17:17938142	AGAGGACCCAGGACT[A/G]CAGGTAGAAATGAGA	146691
rs4257260	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17953689	CACACATGAAGACAC[A/G]TGAGTGGGGGGAGCA	146691
rs4341796	snp	A/C	0.377385	0.215112	intron-variant	TOM1L2	GRCh38.p7	17:17935710	CATCTCTAAAGTCCA[A/C]CAATGATGCCATCAT	146691
rs4343339	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17969275	TTGGTCAGGCTGGCC[C/T]CCAACTCCTGACCTC	146691
rs4413022	snp	C/G	0.448066	0.152544	intron-variant	TOM1L2	GRCh38.p7	17:17954966	CCCTTCCTGACCTCC[C/G]TTTCTTTTGCTGTTG	146691
rs4414547	snp	G/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17955738	actgacttcaagaat[G/T]aagccatagaccctc	146691
rs4458058	snp	A/G	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17910008	cattccagcctaggc[A/G]acagagtaagaccct	146691
rs4470201	snp	A/G	0.455858	0.141853	intron-variant	TOM1L2	GRCh38.p7	17:17941556	GGGATTCCAAGCCAC[A/G]AGGAGATATCCACGG	146691
rs4471742	snp	C/T	0.485392	0.0842056	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974457	GCTCACCGCAACCTC[C/T]GCCTCCCGGTTTCAA	146691
rs4534911	snp	A/G	0.394538	0.203982	intron-variant	TOM1L2	GRCh38.p7	17:17949016	GAAGGGGCCACATAC[A/G]GAGTGACTGTCCCAT	146691
rs4553680	snp	A/G	0.386313	0.209568	intron-variant	TOM1L2	GRCh38.p7	17:17954408	ACCTCAGCCTCCCAG[A/G]TTCAAATGATTCTCC	146691
rs4616339	snp	C/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17952549	ggtgcgtgctgccac[C/G]cctggctaagttttt	146691
rs4616340	snp	C/T	0.448452	0.152042	intron-variant	TOM1L2	GRCh38.p7	17:17958046	AGTAAGTCGAGATTG[C/T]GCCACTGCACTCCAG	146691
rs4621034	snp	C/T	0.42	0.183303	intron-variant	TOM1L2	GRCh38.p7	17:17952381	TCTTTATTTTCTTTt[C/T]ttttttttttttttt	146691
rs4624238	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17954331	TTTTTTTTTTTTTTG[G/T]GATGGAGCTTCGCTT	146691
rs4924822	snp	A/G	0.476401	0.106032	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844699	AAGGCCCATGGTGCC[A/G]GGGGCCCAACTGCAC	146691
rs4924823	snp	A/G	0.484209	0.0874434	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861188	TAGGATTGGAACCCC[A/G]GCTTGCTGTCTGCTC	146691
rs4924824	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17867077	ATATCAACTCTGCCA[C/T]GGCTTCCTCTGTGTG	146691
rs4924825	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17884128	AGGGCTTTGATCCCA[A/G]GGCTGATGGAATCAA	146691
rs4924826	snp	A/C	0.167809	0.236103	intron-variant	TOM1L2	GRCh38.p7	17:17894732	GGTCAGGAATTCAAG[A/C]CCAGCCTAGCCAACA	146691
rs4924827	snp	C/G	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17930247	GCTCCAGAAAGTGGG[C/G]TATAGAGAATTACCA	146691
rs4925120	snp	C/T	0.464416	0.128553	intron-variant	TOM1L2	GRCh38.p7	17:17851319	AGGAAGGCGCTGCCA[C/T]GCAGGCTGATTTTGA	146691
rs4925123	snp	C/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17881060	AGACCTTTAGCTTCT[C/T]AGGGCAGGAACTCAG	146691
rs4925124	snp	A/T	0.147991	0.228242	intron-variant	TOM1L2	GRCh38.p7	17:17887580	CTCCGGGCTCAAGCA[A/T]TCCTCCCACTTTAGC	146691
rs4925125	snp	C/T	0.480853	0.0959518	intron-variant	TOM1L2	GRCh38.p7	17:17891130	CCAGGCAGAAGCTTG[C/T]GAGGCATCTCAAGGC	146691
rs4925126	snp	A/G	0.479904	0.0982045	intron-variant	TOM1L2	GRCh38.p7	17:17895319	TTTCTGACTACCTCA[A/G]TTATTCTCATTTGCC	146691
rs4925127	snp	C/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17903141	TGCCACTGCACTAGT[C/G]TCCGTAGCTATATAT	146691
rs4925128	snp	A/G	0.144632	0.226711	intron-variant	TOM1L2	GRCh38.p7	17:17903636	AAAAAAAAAATGTTG[A/G]GTAAAACAGATGGAA	146691
rs4925129	snp	A/G	0.395635	0.2032	intron-variant	TOM1L2	GRCh38.p7	17:17903872	GGATCTACTTAGTGA[A/G]AGAGGTGACGAGAAC	146691
rs4925130	snp	A/G	0.390651	0.206682	intron-variant	TOM1L2	GRCh38.p7	17:17904544	ATGAGGGGCCTGGTT[A/G]GGGTTTTTAACCTAA	146691
rs4925131	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17904684	AGTGCAGACACCAGA[A/G]AATGCAGCACCTGAC	146691
rs4925132	snp	C/G	0.0248432	0.108648	intron-variant	TOM1L2	GRCh38.p7	17:17904757	CCAATGTCACCCTGT[C/G]TATCCTAGACAGCTT	146691
rs4997327	snp	A/G	0.0448719	0.142907	intron-variant	TOM1L2	GRCh38.p7	17:17920872	AACTCCTGACCTCAG[A/G]TGATCCACCCGCCTC	146691
rs5002487	snp	A/G	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17929146	TATAGTAAAGGGTAC[A/G]AGCCAGAATGCAGTC	146691
rs5819629	in-del	-/A	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17855963	ATATTTGTTGTAAAG[-/A]AAAAAAAAAAAACAA	146691
rs5819630	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17880245	CTCTGAGAGGCTGGG[-/G]CAGTGTCAATAGCAC	146691
rs5819637	in-del	-/T/TT			intron-variant	TOM1L2	GRCh38.p7	17:17938781	TTTTTTTTTTTTTTT[-/T/TT]AATATTTTGTAAAGA	146691
rs5819638	in-del	-/T/TT	0.489142	0.0728777	intron-variant	TOM1L2	GRCh38.p7	17:17954312	TTTTTTTTTTTTTTT[-/T/TT]GTGATGGAGCTTCGC	146691
rs6502618	snp	A/G	0.46137	0.133501	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843427	AGGGTCCCCATGGCC[A/G]CCCCTGCTTAAATAA	146691
rs6502619	snp	C/G	0.377582	0.214995	intron-variant	TOM1L2	GRCh38.p7	17:17876390	CCTGTGGTGGGCTGC[C/G]AAATGCTGCCAAATG	146691
rs6502622	snp	A/G	0.448963	0.151372	intron-variant	TOM1L2	GRCh38.p7	17:17931377	GATCTTTGGAGTCAG[A/G]CCAATTGAGCTCAAA	146691
rs6502624	snp	A/G	0.455977	0.141681	intron-variant	TOM1L2	GRCh38.p7	17:17944622	TCCCCAAAGCACCAG[A/G]CACCTGCTTCTCTTG	146691
rs6502625	snp	C/G	0.346811	0.230494	intron-variant	TOM1L2	GRCh38.p7	17:17944972	CGTACTCCTGACATT[C/G]CAGCAGATGCTGCCC	146691
rs6502626	snp	C/T	0.474363	0.110278	intron-variant	TOM1L2	GRCh38.p7	17:17946136	gcctgcctcagcctc[C/T]gaaagtgctgggatt	146691
rs6502627	snp	C/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17946357	tcctgtacctgttag[C/T]agtcacttcccattc	146691
rs6502629	snp	A/G	0.347914	0.230028	intron-variant	TOM1L2	GRCh38.p7	17:17966328	ACAGGGCCACTGAAT[A/G]AATAAATGAACAAAT	146691
rs7207043	snp	A/G	0.448836	0.15154	intron-variant	TOM1L2	GRCh38.p7	17:17915874	ggttgttaagctgta[A/G]gagttctttatatat	146691
rs7207395	snp	C/T	0.377385	0.215112	intron-variant	TOM1L2	GRCh38.p7	17:17916021	cctgtggttttggta[C/T]catatctcagaaatc	146691
rs7207535	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17964690	ttgagcccagtaggt[C/T]gaggctttaactacg	146691
rs7208190	snp	A/G	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17916343	ctcccaaagtgctgg[A/G]attacaggcatgaat	146691
rs7208950	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17948241	GGATAATCTTGATAC[C/T]AAGATAAATACGCCC	146691
rs7209478	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895399	GGTCCAAGCAAGTGG[A/G]CTTTACCTGGACAAA	146691
rs7209628	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17895473	TGCGACTATATGCCA[A/G]GCACTATGAGAGATC	146691
rs7213225	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17965797	TCAGTCTCTGGCACA[C/T]AGGAATACAACATTA	146691
rs7213566	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17852373	ACTCTGAGCAGGTAT[C/T]TACGATGCCACCAGA	146691
rs7214002	snp	C/G	0.479904	0.0982045	intron-variant	TOM1L2	GRCh38.p7	17:17948790	CCAGAGCAAGGCAGG[C/G]GTCCTAGGAAGGGCT	146691
rs7214028	snp	C/T	0.148996	0.228688	intron-variant	TOM1L2	GRCh38.p7	17:17886872	CCCAAGTTGGGCCAA[C/T]CAGATGCTCCTCCTT	146691
rs7214536	snp	A/G	0.453575	0.145111	intron-variant	TOM1L2	GRCh38.p7	17:17949132	GGTTTCATGCCATGC[A/G]TTTCTCACACAGGAG	146691
rs7214844	snp	A/C	0.0345262	0.126772	intron-variant	TOM1L2	GRCh38.p7	17:17927862	tacagccagggtttc[A/C]ctatgttacccaggc	146691
rs7217349	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17901690	ATGTCTTCAGTTCCT[C/T]CTCTGTGCCCTCTCC	146691
rs7218054	snp	A/G	0.0402882	0.136092	intron-variant	TOM1L2	GRCh38.p7	17:17872132	TCACAATTACTGTAC[A/G]CAGGAAAACCAACAA	146691
rs7218594	snp	A/C	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17910873	tgtgcccagccCCAA[A/C]ACTCTTGATGGTTGG	146691
rs7221575	snp	A/T	0.453209	0.145623	intron-variant	TOM1L2	GRCh38.p7	17:17945290	CACACACACACACAC[A/T]CTCTCTCTCTCTCTC	146691
rs7221934	snp	C/G	0.0770498	0.180522	intron-variant	TOM1L2	GRCh38.p7	17:17863558	GTGGGTGGGAAGACA[C/G]TAGACtttttttttt	146691
rs7222480	snp	G/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17915503	ctattcaattttttt[G/T]gcccctcaccccttt	146691
rs7224621	snp	C/T	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17942296	TCCATTAATAAATAG[C/T]AGTAATAAGGATGGG	146691
rs7224815	snp	A/T	0.337386	0.23423	intron-variant	TOM1L2	GRCh38.p7	17:17942486	CCAGAAAATCATATC[A/T]ATTTAAAGGACATTT	146691
rs7501812	snp	A/G	0.499954	0.00478616	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847593	GTGTCCACGGGGTGC[A/G]AGCGGGGACCCGCCA	146691
rs7503334	snp	C/T	0.377582	0.214995	intron-variant	TOM1L2	GRCh38.p7	17:17876144	ACTGGATGACATAAT[C/T]GCAATCTTTAAAGAT	146691
rs8065076	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17878783	GTGTGGGGCCTTGCA[A/G]TTCACAGCATCCTTC	146691
rs8065416	snp	C/T	0.454664	0.143571	intron-variant	TOM1L2	GRCh38.p7	17:17947848	ATTCATTTTTAATTT[C/T]TTTTGGTAGCATGAG	146691
rs8065497	snp	A/G	0.337158	0.234315	intron-variant	TOM1L2	GRCh38.p7	17:17879335	GCTTGGGTCAAAGAA[A/G]GTTATTTTCTTTTCT	146691
rs8065563	snp	A/G	0.37778	0.214877	intron-variant	TOM1L2	GRCh38.p7	17:17879090	GAATCCTCAGTGTTA[A/G]GGAAAAGCATGGGAG	146691
rs8065970	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17955457	gattctccagcctcc[A/G]tctcccacgtagctg	146691

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